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硅纳米颗粒通过 ROS/Ca/CaMKII 信号通路诱导心脏损伤和功能障碍。

Silica nanoparticles induce cardiac injury and dysfunction via ROS/Ca/CaMKII signaling.

机构信息

Department of Occupational Health and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China.

Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China; Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, China.

出版信息

Sci Total Environ. 2022 Sep 1;837:155733. doi: 10.1016/j.scitotenv.2022.155733. Epub 2022 May 5.

Abstract

Interest is growing to better comprehend the interaction of silica nanoparticles (SiNPs) with the cardiovascular system. In particular, the extremely small size, relatively large surface area and associated unique properties may greatly enhance its toxic potentials compared to larger-sized counterparts. Nevertheless, the underlying mechanisms still need to be evaluated. In this context, the cardiotoxicity of nano-scale (Si-60; particle diameter about 60 nm) and submicro-scale silica particles (Si-300; 300 nm) were examined in ApoE mice via intratracheal instillation, 6.0 mg/kg·bw, once per week for 12 times. The echocardiography showed that the sub-chronic exposure of Si-60 declined cardiac output (CO) and stroke volume (SV), shorten LVIDd and LVIDs, and thickened LVAWs of ApoE mice in compared to the control and Si-300 groups. Histological investigations manifested Si-60 enhanced inflammatory infiltration, myocardial fiber arrangement disorder, hypertrophy and fibrosis in the cardiac tissue, as well as mitochondrial ultrastructural injury. Accordingly, the serum cTnT, cTnI and ANP were significantly elevated by Si-60, as well as cardiac ANP content. In particular, Si-60 greatly increased cardiac ROS, Ca levels and CaMKII activation in comparison with Si-300. Further, in vitro investigations revealed silica particles induced a dose- and size-dependent activation of oxidative stress, mitochondrial membrane permeabilization, intracellular Ca overload, CaMKII signaling activation and ensuing myocardial apoptosis in human cardiomyocytes (AC16). Mechanistic analyses revealed SiNPs induced myocardial apoptosis via ROS/Ca/CaMKII signaling, which may contribute to the abnormalities in cardiac structure and function in vivo. In summary, our research revealed SiNPs caused myocardial impairments, dysfunction and even structural remodeling via ROS/Ca/CaMKII signaling. Of note, a size-dependent myocardial toxicity was noticed, that is, Si-60 greater than Si-300.

摘要

人们越来越感兴趣的是更好地理解纳米二氧化硅颗粒(SiNPs)与心血管系统的相互作用。特别是,由于其非常小的尺寸、相对较大的表面积以及相关的独特性质,与较大尺寸的同类物质相比,其毒性潜力可能大大增强。然而,其潜在的机制仍需要进行评估。在这种情况下,通过气管内滴注方式,在载脂蛋白 E (ApoE) 小鼠中检查了纳米级(Si-60;粒径约 60nm)和亚微米级(Si-300;300nm)的二氧化硅颗粒的心脏毒性,滴注剂量为 6.0mg/kg·bw,每周一次,共 12 次。超声心动图显示,与对照组和 Si-300 组相比,亚慢性暴露于 Si-60 会降低 ApoE 小鼠的心输出量(CO)和每搏输出量(SV),缩短左室舒张末期内径(LVIDd)和左室收缩末期内径(LVIDs),并使左室心壁厚度增加。组织学研究表明,Si-60 增强了心脏组织中的炎症浸润、心肌纤维排列紊乱、肥大和纤维化,以及线粒体超微结构损伤。相应地,Si-60 显著增加了血清肌钙蛋白 T(cTnT)、肌钙蛋白 I(cTnI)和心钠肽(ANP)水平,以及心脏组织中的 ANP 含量。特别是,与 Si-300 相比,Si-60 大大增加了心脏组织的活性氧(ROS)、Ca 水平和钙调蛋白依赖性蛋白激酶 II(CaMKII)的激活。此外,体外研究表明,二氧化硅颗粒诱导的氧化应激、线粒体膜通透性、细胞内 Ca 超载、CaMKII 信号激活以及随之而来的人心肌细胞(AC16)凋亡呈剂量和尺寸依赖性。机制分析表明,SiNPs 通过 ROS/Ca/CaMKII 信号通路诱导心肌细胞凋亡,这可能导致体内心脏结构和功能异常。综上所述,我们的研究表明,SiNPs 通过 ROS/Ca/CaMKII 信号通路导致心肌损伤、功能障碍甚至结构重塑。值得注意的是,观察到了一种依赖于尺寸的心肌毒性,即 Si-60 大于 Si-300。

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